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Purpose: To determine the real-world patterns and extent of potential drug-drug interactions (DDIs) related to nirmatrelvir/ritonavir (NMVr) in China.
Patients And Methods: Data on NMVr-treated patients from over 160 hospitals across 9 Chinese cities from January 2022 to December 2023 were extracted from the Hospital Prescription Analysis (HPA) database, which was established in Beijing in 1997 to promote rational medication use in China. Grade C, D and X DDIs from the Lexicomp database were defined as clinically significant and analyzed in this study. Statistical analyses included descriptive statistics (continuous variables as mean ± SD; categorical variables as counts and percentages) and multivariate binary logistic regression, which was used to identify factors associated with potential DDIs, with adjustment for confounding variables (sex, age, cities, number of co-administered drugs, comorbidities). Analyses were performed using R software (v4.2.2) with < 0.05 as statistically significant, and figures were generated via GraphPad Prism (v10.3.1).
Results: Of 15,567 patients receiving NMVr, the mean age was 62.4 ±18.2 years, and 53.1% were male. 8542 patients received at least one co-administration, and 5391 patients exhibited at least one potential DDI. A total of 10,694 potential DDIs were identified, with a breakdown of 8310 grade C, 2093 grade D and 291 grade X. Systemic corticosteroids (n=3608) and drugs for obstructive airway diseases (n=2220) had the highest frequencies in grade C DDIs, and the lipid modifying agents (n=601) in grade D DDIs, and cardiac therapy drugs (n=130) in grade X DDIs. Co-administration of drugs significantly increased odds of potential DDIs with the risk escalating markedly as the number of drugs increased, and the comorbidities of hypertension (odds ratio [OR]=1.50), asthma (OR=4.28) and mental disorders (OR=7.02) significantly increased it as well.
Conclusion: In this large-scale cross-sectional study in China, approximately one-third of the patients treated with NMVr were at risk of clinically significant potential DDIs, highlighting the importance of making efforts to diminish these risks, such as close monitoring and dose adjustment.
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http://dx.doi.org/10.2147/IDR.S536758 | DOI Listing |
Infect Drug Resist
August 2025
Department of Pharmacy, Beijing Friendship Hospital, Capital Medical University, Beijing, People's Republic of China.
Purpose: To determine the real-world patterns and extent of potential drug-drug interactions (DDIs) related to nirmatrelvir/ritonavir (NMVr) in China.
Patients And Methods: Data on NMVr-treated patients from over 160 hospitals across 9 Chinese cities from January 2022 to December 2023 were extracted from the Hospital Prescription Analysis (HPA) database, which was established in Beijing in 1997 to promote rational medication use in China. Grade C, D and X DDIs from the Lexicomp database were defined as clinically significant and analyzed in this study.
Pigment Cell Melanoma Res
July 2025
Istituto Dermopatico Dell'immacolata, IDI-IRCCS, Rome, Italy.
The unique pharmacokinetics of BRAF and MEK inhibitors make patients vulnerable to drug-drug interactions (DDIs), which may compromise treatment efficacy in metastatic melanoma. This study evaluates the impact of DDIs on clinical outcomes in patients with metastatic melanoma treated with BRAF/MEK inhibitors. This multicenter, observational, retrospective study assessed DDIs using the Drug-PIN software.
View Article and Find Full Text PDFPharmaceuticals (Basel)
April 2025
Clinical Oncology Pharmacy Unit, Lyon Sud Hospital, Hospices Civils de Lyon, 69495 Pierre Bénite, France.
: The multidisciplinary city-hospital Oncoral follow-up of cancer outpatients has been set up to ensure the safety of oral anticancer drugs (OADs). The aim of this study was to assess Oncoral by Relative Dose Intensity (RDI) in patients with hematological malignancies treated with ibrutinib as a model. : The study included all outpatients treated with ibrutinib and followed in Oncoral between January 2016 and June 2020.
View Article and Find Full Text PDFActa Pharm
December 2024
Department of Clinical Pharmacy, University Hospital Dubrava, 10000 Zagreb Croatia.
Cardiovascular diseases (CVDs) are the leading cause of mortality and morbidity globally. It is estimated that 17.9 million people died from CVDs in 2019, which represents 32 % of all deaths worldwide.
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